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Tissue Engineering and Regenerative Medicine ; (6): 66-69, 2016.
Article Dans Anglais | WPRIM | ID: wpr-654675

Résumé

T-vectors are widely used for cloning the polymerase chain reaction (PCR) products. However, the low conversion efficiency of a plasmid into the linear T-vector usually results in non-recombinants. Here, we designed a new plasmid pNBQ-T to easily select the recombinant colonies harboring PCR products. pNBQ-T plasmid, which contains a DsRed indicator gene between two Nt.BspQI restriction cassettes, each of which contains palindromic sequences susceptible to Nt.BspQI nickase (5′-GCTCTTCT


Sujets)
Clones cellulaires , Clonage d'organisme , Deoxyribonuclease I , Méthodes , Myostatine , Plasmides , Réaction de polymérisation en chaîne
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